Have questions? Visit https://www.reddit.com/r/SNPedia

rs143961508

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs143961508(C;C)
Make rs143961508(C;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356803
GeneHLA-B
is asnp
is mentioned by
dbSNPrs143961508
ebirs143961508
HLIrs143961508
Exacrs143961508
Varsomers143961508
Maprs143961508
PheGenIrs143961508
hapmaprs143961508
1000 genomesrs143961508
hgdprs143961508
ensemblrs143961508
gopubmedrs143961508
geneviewrs143961508
scholarrs143961508
googlers143961508
pharmgkbrs143961508
gwascentralrs143961508
openSNPrs143961508
23andMers143961508
23andMe allrs143961508
SNP Nexus

SNPshotrs143961508
SNPdbers143961508
MSV3drs143961508
GWAS Ctlgrs143961508
GMAF0.02112
Max Magnitude0
ClinVar
Risk rs143961508(C;C)
Alt rs143961508(C;C)
Reference rs143961508(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 0
HGVS NC_000006.11:g.31324580T>C
CLNSRC
CLNACC